Canonical Allele Identifier: CA381579687

Gene: TCIRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68044130A>C , CM000673.2:g.68044130A>C	GRCh38
NC_000011.9:g.67811597A>C , CM000673.1:g.67811597A>C	GRCh37
NC_000011.8:g.67568173A>C	NCBI36
NG_007878.1:g.10115A>C , LRG_115:g.10115A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006019.4:c.808-2A>C MANE Select	NP_006010.2:n.808-2A>C
ENST00000265686.8:c.808-2A>C MANE Select	ENSP00000265686.3:n.808-2A>C
NM_001351059.1:c.-87-2A>C	NP_001337988.1:n.-87-2A>C
NM_001351059.2:c.-87-2A>C	NP_001337988.1:n.-87-2A>C
NM_006019.3:c.808-2A>C	NP_006010.2:n.808-2A>C
NM_006053.3:c.160-2A>C	NP_006044.1:n.160-2A>C
NM_006053.4:c.160-2A>C	NP_006044.1:n.160-2A>C
ENST00000265686.7:c.808-2A>C	ENSP00000265686.3:n.808-2A>C
ENST00000524598.5:c.766-2A>C	ENSP00000432846.1:n.766-2A>C
ENST00000525724.5:n.120-2A>C
ENST00000527530.1:n.426-2A>C
ENST00000529364.1:c.308-2A>C
ENST00000532635.5:c.160-2A>C	ENSP00000434407.1:n.160-2A>C
ENST00000534673.5:c.*156-2A>C	ENSP00000431174.1:n.*156-2A>C
ENST00000698254.1:c.404-69A>C	ENSP00000513629.1:n.404-69A>C
ENST00000698255.1:c.757-2A>C	ENSP00000513630.1:n.757-2A>C
ENST00000698256.1:c.274-2A>C
ENST00000698257.1:n.226-2A>C
XM_005273709.2:c.808-2A>C	XP_005273766.1:n.808-2A>C
XM_011544726.1:c.808-2A>C	XP_011543028.1:n.808-2A>C
XM_011544727.1:c.808-2A>C	XP_011543029.1:n.808-2A>C
XM_011544728.1:c.808-2A>C	XP_011543030.1:n.808-2A>C
XM_011544729.1:c.824-2A>C	XP_011543031.1:n.824-2A>C
XM_024448320.1:c.824-2A>C	XP_024304088.1:n.824-2A>C
XM_024448321.1:c.824-2A>C	XP_024304089.1:n.824-2A>C
XM_024448322.1:c.824-2A>C	XP_024304090.1:n.824-2A>C
XM_024448323.1:c.824-2A>C	XP_024304091.1:n.824-2A>C
XM_024448324.1:c.824-2A>C	XP_024304092.1:n.824-2A>C
XR_001747721.2:n.932-2A>C
XR_001747722.1:n.945-2A>C
XR_001747723.2:n.945-2A>C
XR_002957115.1:n.946-2A>C
XR_949754.1:n.812-2A>C